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An observational study of haemophilia A patients without inhibitors using the French national claims (SNDS) database.
Trossaërt, Marc; Falk, Aletta; Gautier, Laurène; Kragh, Nana; Van Hinloopen, Olivia; Varin, Remi.
Afiliação
  • Trossaërt M; Hemophilia Treatment Centre, University Hospital of Nantes, Nantes, France.
  • Falk A; Global Medical Affairs and Clinical Science, Sobi, Stockholm, Sweden.
  • Gautier L; Real World Evidence Data and Analytics, Cerner Enviza, Paris, France.
  • Kragh N; Global Health Economics and Outcomes Research, Sobi, Stockholm, Sweden.
  • Van Hinloopen O; Patient Access, Sobi, Paris, France.
  • Varin R; Department of Pharmacy, Rouen University Hospital, Rouen, France.
Hematology ; 29(1): 2320610, 2024 Dec.
Article em En | MEDLINE | ID: mdl-38445826
ABSTRACT

OBJECTIVES:

To describe clinical characteristics, factor consumption, and events of interest in patients with haemophilia A without inhibitors receiving prophylaxis in France, and the clinical impact of switching to Elocta® in this population.

METHODS:

This retrospective, observational study using the Système National des Données de Santé database, analysed data from patients with haemophilia A without inhibitors using prophylactic factor VIII (FVIII) replacement therapy during 2016-2019. Clinical characteristics, treatment patterns and switches, factor consumption, and rate of events of interest were determined. In a sub-cohort of patients treated with Elocta®, clinical characteristics, factor consumption, and rate of events of interest before and after switching to Elocta® were compared.

RESULTS:

For 545 patients, with mean age (standard deviation [SD]) 25.4 (17.8) years, Elocta® was the most used treatment. Bleeding events and articular non-bleeding events leading to hospitalization occurred in 15.4% and 13.9% of patients, respectively, and 9.9% of patients had surgeries or procedures related to haemophilic arthropathy. The mean (SD) FVIII product consumption was 344 (93) IU/kg/month for extended half-life treatment, and 331 (98) IU/kg/month for standard half-life products. For the sub-cohort of 146 patients, bleeding events (SD) decreased from 0.32 (2.2) to 0.09 (0.42) events/patient/year (p = 0.227) after switching to Elocta®. There was no statistically significant difference in rates of factor consumption or articular non-bleeding events before and after initiation of Elocta®.

CONCLUSION:

This study provides real-world insights that advance the understanding of treatment patterns and events of interest in patients with haemophilia A on prophylactic regimens in France.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemofilia A Limite: Adult / Humans Idioma: En Revista: Hematology Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemofilia A Limite: Adult / Humans Idioma: En Revista: Hematology Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França
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